Zobrazeno 1 - 10
of 1 980
pro vyhledávání: '"Pearce G"'
Autor:
Alessandro N. Franciosi, April Tanzler, Jodi Goodwin, Pearce G. Wilcox, George M. Solomon, Albert Faro, Noel G. McElvaney, Damian G. Downey, Bradley S. Quon
Publikováno v:
ERJ Open Research, Vol 8, Iss 4 (2022)
Background Increasing awareness of milder presentations of cystic fibrosis (CF) and greater interest in non-CF bronchiectasis are likely to lead to more CF screening by respiratory clinicians. As a result, adults who may not strictly fulfil CF diagno
Externí odkaz:
https://doaj.org/article/6f617089f9e54fb9bd7aabebc4efc679
Autor:
Tao Chen, Amy Po Yu Tsai, Seo Am Hur, Alyson W. Wong, Mohsen Sadatsafavi, Jolene H. Fisher, Kerri A. Johannson, Deborah Assayag, Julie Morisset, Shane Shapera, Nasreen Khalil, Charlene D. Fell, Helene Manganas, Gerard Cox, Teresa To, Andrea S. Gershon, Nathan Hambly, Andrew J. Halayko, Pearce G. Wilcox, Martin Kolb, Christopher J. Ryerson
Publikováno v:
Respiratory Research, Vol 22, Iss 1, Pp 1-9 (2021)
Abstract Rationale The University of California, San Diego Shortness of Breath Questionnaire (UCSDSOBQ) is a frequently used domain-specific dyspnea questionnaire; however, there is little information available regarding its use and minimum important
Externí odkaz:
https://doaj.org/article/02be01e682484773ab03379e97c4b7ef
Autor:
Alyson W. Wong, Tae Yoon Lee, Kerri A. Johannson, Deborah Assayag, Julie Morisset, Charlene D. Fell, Jolene H. Fisher, Shane Shapera, Andrea S. Gershon, Gerard Cox, Andrew J. Halayko, Nathan Hambly, Helene Manganas, Mohsen Sadatsafavi, Pearce G. Wilcox, Teresa To, Veronica Marcoux, Nasreen Khalil, Martin Kolb, Christopher J. Ryerson
Publikováno v:
Respiratory Research, Vol 21, Iss 1, Pp 1-9 (2020)
Abstract Background Comorbidities are frequent and have been associated with poor quality of life, increased hospitalizations, and mortality in patients with interstitial lung disease (ILD). However, it is unclear how comorbidities lead to these nega
Externí odkaz:
https://doaj.org/article/20adba84a4ee4ef69531905b9f1bdd30
Autor:
Bradley S. Quon, Andrew H. Ramsook, Satvir S. Dhillon, Reid A. Mitchell, Kyle G. Boyle, Pearce G. Wilcox, Jordan A. Guenette
Publikováno v:
Respiratory Research, Vol 21, Iss 1, Pp 1-4 (2020)
Abstract Rationale Lumacaftor/ivacaftor (LUM/IVA) modestly improves lung function following 1 month of treatment but it is unknown if this translates into improvements in exercise endurance and exertional symptoms. Methods Adult CF participants compl
Externí odkaz:
https://doaj.org/article/4b861c2f63ec4e6386752372ee3caecf
Publikováno v:
Respiratory Medicine Case Reports, Vol 40, Iss , Pp 101778- (2022)
The introduction and rapid uptake of CFTR modulator therapy, in addition to other treatments, has significantly increased life expectancy in CF and provided more women the opportunity to consider and successfully be managed throughout pregnancy. Ther
Externí odkaz:
https://doaj.org/article/f8af1215684040839001f3998c9239ed
Publikováno v:
BMC Pulmonary Medicine, Vol 19, Iss 1, Pp 1-9 (2019)
Abstract Background Connective tissue disease-associated interstitial lung disease (CTD-ILD) is associated with reduced quality of life and poor prognosis. Prior studies have not identified a consistent combination of variables that accurately predic
Externí odkaz:
https://doaj.org/article/a754ad4cd3934b07a2c7746a442b2fb5
Publikováno v:
ERJ Open Research, Vol 7, Iss 1 (2021)
Sex differences in morbidity and mortality have been reported in the cystic fibrosis (CF) population worldwide. However, it is unclear why CF women have worse clinical outcomes than men. In this review, we focus on the influence of female sex hormone
Externí odkaz:
https://doaj.org/article/8a1f0a3eb8f84247aec28a87fe8364d1
Autor:
Bradley S Quon, Pearce G Wilcox
Publikováno v:
Canadian Respiratory Journal, Vol 22, Iss 5, Pp 257-260 (2015)
The gene responsible for cystic fibrosis (CF) was discovered 25 years ago. This breakthrough has enabled a sophisticated understanding of how various mutations lead to specific alterations in the structure and function of the CF transmembrane regulat
Externí odkaz:
https://doaj.org/article/48e7c668025e4cf0a27b35b0ea29adf6
Publikováno v:
Canadian Respiratory Journal, Vol 20, Iss 5, Pp 335-338 (2013)
Immunoglobulin (Ig) G4-related lung disease is a fibroinflammatory entity that presents in protean ways. Diagnostically, IgG4-related lung disease requires a high clinical index of suspicion complemented by elevated serum IgG4 levels and/or biopsy th
Externí odkaz:
https://doaj.org/article/8bb12f87bb3e4bcf982a6eb6df65feeb